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European Journal of Nuclear Medicine and Molecular Imaging|December 14, 2019
Succinate detection using in vivo <sup>1</sup>H-MR spectroscopy identifies germline and somatic SDHx mutations in paragangliomasCharlotte Lussey-Lepoutre, Alexandre Bellucci, Nelly Burnichon, et al.
Molecular and Cellular Biology|November 17, 2005
Muscle-specific loss of apoptosis-inducing factor leads to mitochondrial dysfunction, skeletal muscle atrophy, and dilated cardiomyopathyNicholas Joza, Gavin Y Oudit, Doris Brown, et al.
Scientific Reports|June 6, 2020
miR-379 links glucocorticoid treatment with mitochondrial response in Duchenne muscular dystrophyMathilde Sanson, Ai Vu Hong, Emmanuelle Massourides, et al.
The Journal of Pediatrics|September 13, 2003
Antenatal manifestations of mitochondrial respiratory chain deficiencyJürgen-Christoph von Kleist-Retzow, Valérie Cormier-Daire, Géraldine Viot, et al.
Cell Metabolism|June 7, 2007
S6 kinase deletion suppresses muscle growth adaptations to nutrient availability by activating AMP kinaseVictor Aguilar, Samira Alliouachene, Athanassia Sotiropoulos, et al.
Cell|November 6, 2007
Targeted deletion of AIF decreases mitochondrial oxidative phosphorylation and protects from obesity and diabetesJ Andrew Pospisilik, Claude Knauf, Nicholas Joza, et al.
Cancer Cell|May 28, 2013
SDH mutations establish a hypermethylator phenotype in paragangliomaEric Letouzé, Cosimo Martinelli, Céline Loriot, et al.
Plos One|September 19, 2009
The Warburg effect is genetically determined in inherited pheochromocytomasJudith Favier, Jean-Jacques Brière, Nelly Burnichon, et al.
Pediatric Nephrology (Berlin, Germany)|February 1, 2005
Respiratory chain deficiency presenting as congenital nephrotic syndromeAlice Goldenberg, Linh Huynh Ngoc, Marie-Christine Thouret, et al.
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